Nasal Chondromesenchymal Hamartoma (NCMH): a systematic ...

Mason et al. Journal of Otolaryngology - Head and Neck Surgery (2015) 44:28 DOI 10.1186/s40463-015-0077-3

ORIGINAL RESEARCH ARTICLE

Open Access

Nasal Chondromesenchymal Hamartoma (NCMH): a systematic review of the literature with a new case report Katrina Anna Mason1* , Annakan Navaratnam2, Evgenia Theodorakopoulou1 and Perumal Gounder Chokkalingam2

Abstract Background: Nasal chondromesenchymal hamartoma (NCMH) is a very rare, benign tumour of the sinonasal tract usually presenting in infants. We present a systematic review of NCMH cases alongside a case report of an adult with asymptomatic NCMH. Methods: A systematic review was conducted in accordance with PRISMA guidelines. A PubMed, EMBASE and manual search through references of relevant publications was used to identify all published case-reports of NCMH. Data was collected from each case-report on: patient demographics, laterality, size and location of NCMH, presentation, co-morbidities, investigations, treatment and follow-up. Results: The systematic review identified 48 patients (including ours): 33 male, 15 female. Mean age was 9.6 years (range: 1 day–69 years) with the majority aged 1 year or younger at presentation (n = 18). Presentations included: nasal congestion (n = 17), nasal mass (n = 15) and eye signs (n = 12). NCMH also involved the paranasal sinuses (n = 26), orbit (n = 16) and skull-base (n = 14). All patients underwent operative resection of NCMH. A small 2014 case-series found DICER1 mutations in 6 NCMH patients, establishing a link to the DICER1 tumour spectrum. Conclusions: NCMH is a rare cause of nasal masses in young children and adults. In light of the newly established link between NCMH and DICER1 mutations surgeons should be vigilant for associated DICER1 tumours, as NCMH may be the ‘herald tumour’ of this disease spectrum. Keywords: Nasal neoplasms, Hamartoma, DICER1 protein human, Review

Background Nasal chondromesenchymal hamartoma (NCMH) is a very rare, benign tumour of the sinonasal tract. Fortyseven cases have been reported in the English literature and the vast majority of these presentations are in infants and young children often below the age of one. NCMHs have a mixed morphological structure comprised of predominantly mesenchymal and cartilaginous components. NCMH patients present with symptoms that are dependent on the location of the tumour in the nasal cavity or paranasal sinuses and their compression of local structures. These symptoms range from nasal obstruction to visual impairment and facial and dental * Correspondence: [email protected] 1 Barts and The London School of Medicine and Dentistry, The Blizard Institute of Cell and Molecular Science, 4 Newark Street, Whitechapel, E1 2AT London, UK Full list of author information is available at the end of the article

pain. To date there have only been 6 cases of adult presentation of NCMH. Here we present the first systematic review of NCMH cases published in the literature to assess the patient demographics, presentation, management and prognosis of NCMH alongside a new and unusual case in an adult.

Case report

A 49-year-old man was referred to our outpatient clinic presenting with a small mass in his right nasal cavity. The lump, which the patient first noticed 5 years ago, had been growing insidiously over time and by the time of presentation had become visible at the right anterior naris. The patient did not complain of any symptoms but sought consultation as his wife was concerned by the cosmetic appearance of the mass.

© 2015 Mason et al. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http:// creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Mason et al. Journal of Otolaryngology - Head and Neck Surgery (2015) 44:28

Examination revealed a large firm mass arising from the right side of the anterior nasal septum with approximately 0.5 cm attachment to the anterior cartilage of the septum. The left and right nasal cavities were otherwise unremarkable. Clinically, the mass had the appearance of a papilloma confined to the nasal cavity with an attachment to the septum only and therefore further imaging was not undertaken. The differential diagnoses considered at the time of presentation were: nasal polyp, squamous papilloma or inverted papilloma. The patient subsequently underwent excisional biopsy of the right nostril mass under general anaesthetic using a circumferential subperichondrial incision with a small margin. Intraoperatively, the mass had the macroscopic appearance of a 0.5 cm × 2 cm × 2 cm calcified nodule. Due to a small 0.5 cm base, subsequent healing was achieved by secondary intention aided by the routine application of topical antibacterial cream. Histopathological analysis showed the nodule to contain cartilage and aneurysmal bone covered in stratified squamous epithelium with keratinisation (Figs. 1 and 2). Histopathological diagnosis was made using a haematoxylin & eosin stain. These findings were consistent with a diagnosis of a nasal chondromesenchymal hamartoma. The patient was followed up in clinic and was discharged after 2 years having shown no signs of recurrence. Furthermore, a telephone interview was conducted 4 years post operation and the patient reported no recurrence of the nasal mass. He confirmed that he had no postoperative complications and was happy with the outcome of the operation.

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Methods A systematic review was undertaken in accordance with PRISMA guidelines [1]. No systematic review protocol was used, however our systematic review methodology is described below and a four-phase flow diagram is represented in Fig. 3. All published case-reports of NCMH were included in the review. A PubMed search (MEDLINE) (1975 to May Week 2, 2015) was carried out using the following terms [(chondromesenchymal hamartoma) AND (nasal OR sinus OR maxillary OR ethmoid OR sphenoid OR frontal OR orbit OR cranial)]. An EMBASE search (1975 to May Week 2, 2015) was carried out using a best sensitivity-combination strategy. The PubMed search resulted in 32 citations of which 24 were relevant, 6 were not NCMH case-reports, one was a Chinese language casereport, and one case was a duplicate case-report publication [2]. An EMBASE search and a manual search through references of relevant publications yielded 11 further relevant citations. Of these only 6 were included in the analysis; one case was found to have been a duplicate case report [3, 4] and four other possible cases of NCMH were found through publication citation search, but were labelled as “Mesenchymal chondrosarcoma” [5] “nasal hamartoma” [6], “nasopharyngeal hamartoma” [7], and “congenital mesenchymoma” [8], and were therefore not included. Thirty-one publications that report 47 cases of NCMH were included in this systematic review. Data was collected on patient demographics (age, gender), laterality, size and site of NCMH, presentation, co-morbidities, investigations, treatment and follow-up. These were also the principle summary measures. Two

Fig. 1 Nodule containing cartilage and aneurysmal bone and covered by stratified squamous epithelium with keratinisation (magnification ×25, haematoxylin & eosin stain)


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Fig. 2 Areas of osteoid formation (magnification ×200, haematoxylin & eosin stain)

8

Fig. 3 Four-phase flow diagram of systematic review in accordance with PRISMA guidelines * Two individual publications of single case-reports were excluded from analysis as these had previously been published, Schultz et al. [2] and Kang et al. [3].** See Table 1


authors performed the database search, the manual search through references of relevant publications, and extracted the relevant data from the case-reports. Data was entered into an Excel 2013 Microsoft Office™ database which was used to carry out basic statistical analysis. Results of systematic review

Forty-Eight NCMH patients (including our case) have been reported in the English literature (Fig. 3). Most cases presented in males; 33 male and 15 female, with a male to female ratio of 2.2:1 ratio. The mean age was 9.6 years (range: 1 day–69 years). A large proportion of these patients were aged 1 year or younger at presentation (n = 18) and only 8 adult patients (including our case) have been described. Site of pathology was limited to the nasal cavity only in 10 patients, and involved the paranasal sinuses (maxillary, ethmoid, sphenoid) in 26 patients, the orbit in 16 patients, extending to the skull base in 14 patients, had intracranial extension in 8 cases, involved the nasopharynx in 3 patients and the oropharynx in 2 patients (see Table 1). Clinical presentations of NCMH patients included: nasal congestion or obstruction (n = 17), nasal mass (n = 15), eye signs (proptosis, hypotropia, enopthalmos, strabismus, exotropia etc.) (n = 12), facial swelling (n = 8), headaches or facial pain (n = 6), stertor or respiratory distress (n = 8), ophthalmoplegia (n = 4), recurrent sinusitis (n = 4), rhinorrhoea (n = 3), otitis media (n = 2), epistaxis (n = 2), toothache (n = 1), hyposmia (n = 1), hydrocephalus (n = 1) and 4 patients were asymptomatic or had no signs and symptoms documented (see Table 1). All patients underwent operative resection of NCMH and the surgical approach was dependent on disease location. One patient had pre-operative chemotherapy due to initial misdiagnosis on biopsy as spindle cell sarcoma. One patient had pre-operative embolization to reduce operative blood loss. Follow up times were included for 24 patients, mean time for follow-up was 24 months, (range 2–156 months). Eleven patients were found to have persistent disease or disease recurrence on follow up, seven required further surgery, three patients were described as stable, and no further information was given on the other patient. Li et al. described the first and only reported case of malignant transformation of NCMH [9]. Thirty-six patients had no documented past medical problems. One adult patient had a history of multiple vascular aneurysms. Eleven of the patients had been diagnosed with pleuropulmonary blastoma (PPB) prior to NCMH detection. Of these 11 patients, 5 had other comorbidities including three with Sertoli-Lleydig cell ovarian tumours, two with pulmonary cysts, one jejunal polyps, one papillary thyroid carcinoma, one cystic nephroma and one multinodular goitre.

Page 4 of 14

A potential weakness of this systematic review is the possibility of reporting bias through publication bias both within individual case reports and across the review. This reporting bias is three-fold: firstly in the incomplete publication of all the clinical aspects of the case-reports by the original authors, for example not reporting follow-up times or co-morbidities etc. Secondly it is possible that there have been cases of NCMH that have not been reported in the literature and can therefore not be included in the systematic review. Thirdly the exclusion of case-reports of “Mesenchymal chondrosarcoma” [5] “nasal hamartoma” [6], “nasopharyngeal hamartoma” [7], and “congenital mesenchymoma” [8] alongside others, which are published prior to the first description of NCMH by McDermot et al. in 1998, may have resulted in an underreporting of true NCMH cases. However without being able to retrospectively assess and re-classify the histology of these cases we feel it is appropriate to have excluded them from our analysis and conclusions. These sources of reporting biases could potentially reduce the validity of conclusions drawn in terms of not fully representing or capturing all possible cases of NCMH.

Discussion NCMHs are predominantly benign lesions that are locally destructive and because of their aggressive appearance can be mistaken for a malignant tumour. However NCMHs can be slow growing and therefore have a delayed presentation. Histopathologically these lesions are analogous to other mesenchymal hamartomas, and consist of islands of chondroid tissue such as hyaline cartilage, areas of calcification, and mesenchymal cellular elements such as spindle cells and myxoid stroma. McDermott et al. were the first to recognise NCMH as a distinct clinic-pathological entity in 1998 when they described a case series of seven patients with a tumefactive process of the nasal passages and contiguous paranasal sinuses with a detectable mass in the nose [10]. In this case series, six of the seven patients were infants under the age of 3 months. As our systematic review demonstrates NCMH predominantly presents in young children and infants under the age of one, but there have now been seven case reports, including ours, of adults with NCMH up to the age of 69 [9, 11–14]. In 2013 the first and only reported case of malignant transformation of an NCMH was described in the literature [9]. In our case, the NCMH was initially thought to be a papilloma confined to the nasal septal wall and therefore further imaging was not undertaken prior to resection. However pre-operative imaging of these lesions provides valuable information regarding involvement of adjacent structures such as the paranasal sinuses, orbit and intracranial cavity. On computed tomography (CT) imaging,

Author, Publication date

Case No

Age D/M/Y

Sex Side & Size

Site

Symptoms

Co-morbidity

Investigations Treatment

Follow Up/

(1) McDermot, 1998 [10] USA

1

5D

M

1. Nasal cavity

1. Nasal Mass

ND

CT

Surgical excision

No recurrence at2 years

ND

MRI

Surgical excision

No recurrence at 2 years

ND

ND

Biopsy then surgical excision Subsequent chemotherapy


1. Nasal Mass

ND

ND

Surgical excision

No recurrence at 18 months

1. Nasal Mass

ND

CT

Surgical excision & further re-excision after 16 months

Unchanged persistent tumour in superior nasal cavity at 12 months

1. Nasal cavity

1. Nasal Mass

ND

CT

2. Ethmoid sinus

2. Hydrocephalus & agenesis of corpus callosum

Surgical excision VP shunt for hydrocephalus

Residual tumour in anterior cranial fossa at 9 months

PPB

ND

Surgical excision

No recurrence at 2 months NB later reported by Priest et al. 2010 [27]- showed with multiple recurrences in first 3 years

ND

CT

Surgical excision

ND

None stated

CT MRI

Surgical excision with mid-facial de-gloving and bi-frontal craniotomy


None stated

CT

Two stage surgical excision 1st intracranial/sinus


ND

2. Respiratory Difficulties 2

3M

F

ND

1. Nasal cavity

1. Nasal Mass

2. Ethmoid Sinus

2. Otitis Media

3. Intracranial extension 3

3M

M

ND

1. Nasal cavity

1. Choanal Mass 2. Respiratory distress

4

2M

M

ND

1. Nasal cavity 2. Intracranial extension

5

12 D

F

ND

1. Nasal cavity 2. Intracranial extension

6

14 D

M

ND

3. Intracranial extension 7

(2) Chae 1999 Korea [30] *abstract only, Korean paper

8

(3) Kim D 1999 [31] USA

9

(4) Kato, 1999 [17] Japan

10

7Y

3M

M

F

ND

1. Nasal cavity

1. Nasal Mass

2. Sphenoid sinus

2. Nasal Congestion

Right Size: 3.5 × 7.5 × 2.5 cm

1. Nasal cavity

1. Epistaxis

2. Ethmoid sinus

2. Obstruction

Right Size: ND

1. Nasal cavity

1. Nasal mass

2. Intracranial extension

2. Otitis media


Table 1 Summary table of systematic review of NCMH cases reported in the literature

3. Cribriform plate 3M

F

3. Ethmoid sinus M

Left Size: ND

1. Nasal cavity

1. Nasal Mass


2. Respiratory distress with cyanosis when feeding

Page 5 of 14

4M

lesion, 2nd intranasal lesion

(5) Hsueh 2001 [32] Taiwan (2 cases)

11

0D

M

Left Size: ND

3. Extension to left orbit

3. Opthalmoplegia left eye

1. Nasal cavity

1. Left facial swelling

1. Sphenoid sinus

2. Left nasal mass

3. Ethmoid sinus

3. Respiratory distress & cyanosis when feeding

4. Compression of left orbit

Radiotherapy post op None stated

CT MRI

Excision biopsy then subsequent surgical excision with lateral rhinotomy and craniofacial approach

Recurrence after excision biopsy No recurrence at 5 years after second surgery

None stated

CT MRI

Surgical resection


4. Proptosis on recurrence 12

9M

M

Right ND

1. Nasal cavity

1. Asymmetric face

2. Maxillary sinus

2. Right opthalmoplegia, enopthalmos and hypotropia

(6) Alrawi 2003 [14] Ireland

13

16 Y

M

Left 1.5 × 1.5 cm

1. Nasal cavity

1. Nasal swelling

None stated

CT MRI

Surgical resection with delayed reconstruction with forehead flap


(7) Shet, 2004 [21] India

14

1Y

M

Left Size: ND

1. Nasal cavity

1. Proptosis of left eye

Non stated

CT

2. Extension into left orbit

2. Left facial swelling

Chemotherapy (VID) as biopsy suggested spindle cell sarcoma30 % reduction in tumour size Then Left maxillectomy and surgical excision

Residual tumour at 1.5 years near eye but no further re-growth & stable

1. Left eye ptosis

None stated

CT

Frontal craniotomy & trans-nasal surgical resection

ND

1. Headaches left sided

None stated

CT

Endoscopic biopsy and anterior craniofacial resection

ND

1. Nasal mass

None stated

ND

Surgery and care undertaken in another hospital

ND Surgery and care undertaken in another hospital

3. Ethmoid sinus 4. Sphenoid sinus (8) Kim B, 2004 [22] Korea

15

5M

M

Left Size: ND

1. Nasal cavity 2. Compression of left orbit


Table 1 Summary table of systematic review of NCMH cases reported in the literature (Continued)

3. Defect left ethmoidal bone 4. Defects anterior cranial fossa 16

(10) Ozolek, 2005 [11] USA (4 cases)

17

11 Y

M

Left Size: ND

1. Nasal cavity 2. Displacement left orbital wall

11 Y

M

Left Size: ND

1. Nasal cavity 2. Ethmoid sinus 3. Extension into left orbit

Page 6 of 14

(9) Norman, 2004 [15] USA

18

17 Y

F

ND Size: ND

1. Nasal cavity

19

25 Y

M

Bilateral 8 × 5 × 3.5 cm

1. Nasal cavity

1. Nasal obstruction

None stated

ND

Surgical excision

ND

CT

Multiple surgical resections within one year including, tracheostomy and initial surgical resection, further surgical resection of bulbar mass and nasal tumour, then Le-Fort osteotomy and further surgical resection

ND

2. Facial pain

2. Oropharynx

2. Chronic sinusitis

1. Nasal cavity

ND

None stated

ND

Surgical excision

ND

1. Nasal Obstruction

None stated

CT

Surgical excision


CT

Endoscopic surgical excision


None stated

CT MRI

Surgical resectionright lateral rhinotomy


3. Nasopharynx

20

69 Y

F

Right Size: ND

1. Respiratory distress from obstructing oropharyngeal tumour requiring emergency tracheostomy

1. Multiple Intracranial vascular aneurysms 2. Longstanding nasopharyngeal tumour- biopsy aged 13 ‘chronic inflamed polyp’

2. Maxillary sinus

2. Ethmoid sinus (11) Low 2006 [33] UK

21

11 Y

M

Right Size: ND

1. Nasal cavity

2. Epistaxis (12) Johnson, 2007 [29] USA

22

15 Y

F

Bilateral Size: ND

1. Nasal cavity


1. PPB

2. Nasopharynx

2. Chronic sinusitis

2. Sertoli-Leydig cell Ovarian Tumour



3. Congenital phthisi bulbi (13) Silkiss, 2007 [18] USA

23

24

(15) Finitsis, 2009 [35] Greece

25

12 Y

M

M

Right 3.2 × 1.4 cm

Left 1.5 cm

1. Nasal cavity

1. Ptosis

2. Erosion of cribriform plate

2. Extropia

3. Compression of right orbit

3. Strabismus 4. Stertor

1. Nasal cavity


None stated

CT

Endoscopic surgical resection and further endoscopic surgical resection after recurrence

Recurrence at 2 months No recurrence at 5 months post second surgery

1. Respiratory distress

None stated

CT MRI

Pre-operative embolization Then Surgical resection with midface de-gloving

ND

2. Sphenoid sinus 3. Ethmoid sinus 4. Maxillary sinus 12 M

M

Left 4 cm × 4.2 cm

1. Nasal cavity 2. Compression of left orbit 3. Maxillary sinus compression

Page 7 of 14

(14) Nakagawa 2008 [34] Japan

7M

4. Nasopharynx (16) Kim J, 2009 [23] Korea

26

19 M

M

Left 2.7 × 3.5 cm

1. Nasal cavity

1. Watery rhinorrhoea

2. Orbital extension


3. Intracranial extension (17) Priest, 2010 [27] USA *case previously reported by McDermot et al. 1998 **case previously reported by Johnson et al. 2007 (2 new cases)

-

-

7Y*

15 Y **

M

F

Initially unilateral, then bilateral

Bilateral

1. Sphenoid sinus

1. Nasal Congestion

1. PPB type II–III

2. Left Nasal cavity

2. Nasal mass

2. Lung cysts

1. Bilateral nasal cavities

1. Chronic Sinusitis

1. PPB Type II

2. Bony erosion of posterior septum

2. Facial Pain

2. Sertoli-Leydig Cell Ovarian Tumour

2. Extending into nasopharynx

3. Nasal Congestion

3. Congenital phthisi bulbi Stickler syndrome


CT MRI

Endoscopic surgical resection ×2

Recurrence at one year; 2nd surgery. No recurrence 10 months after second surgery

Four resections over 3 years

Followed up for 13 years with multiple recurrences in first 3 years

Surgical resection


27

10 Y

F

Bilateral Size: ND



1. PPB Type III

CT

Surgical resection


28

11 Y

M

Right Size: ND

1. Nasal cavity


1. PPB Type III

ND

Surgical resection


ND

MRI

Biopsy and then lateral rhinotomy for excision

ND

None stated

CT MRI

Endoscopic surgical resection

ND

None stated

CT MRI


ND

2. Extension to anterior skull base (18) Sarin, 2010 [24] India

None stated

29

2.5 Y

M

Right Size: ND

1. Nasal cavity

1. Right eye oculomotor 2. Maxillary, ethmoid impairment and sphenoid sinus



3. Erosion of middle wall of orbit (19) Eloy 2011 [25] Belgium

31

18 M*

7D

M

F

Right 0.5 × 0.4 cm

Right Size: ND

1. Nasal cavity


2. Ethmoid sinus

2. Nasal mass

3. Extension into right orbit

3. Hypertelorism, proptosis, diplopia


4. Nasal swelling *symptoms 1st noticed at 2 months- delayed referral from Algeria to Brussels

1. Nasal cavity

1. Nasal Mass 2. Stertor

Page 8 of 14

(20) Jeyakumar 2011 [26] USA

30

3. Proptosis right eye (21) Mattos 2011 [20] USA

32

3Y

M

Left Size : ND

1. Nasal cavity

1. Eye infections

2. Ethmoid sinus

2. Eye congestion



4. Left maxilla

4. Cheek fullness

None stated

CT MRI

Endoscopic excision the Recurrence at 21 further surgical excision months required further resection

5. Intermitted left eye/face pain (22) Behery, 2012 [36] USA

33

11 Y

M

ND

ND

Nasal Obstruction

1. PPB

(23) 34 Uzomefuna, 2012 [37] Ireland

8Y

M

ND

1. Sphenoid sinus

1. Frontal Headache

ND

(24) Cho, 2013 [4] Korea

14 Y

1. Nasal cavity

1. Swelling and pain to left face

2. Maxillary sinus

2. Tooth mobility

35

2. Ethmoid sinus M

Left 5 cm × 5.3 cm × 4 cm

Surgical resection

ND

CT MRI

Endoscopic surgical resection


None stated

CT

Subtotal maxillectomy, No recurrence at removal or orbital floor, 4 years removal of medial nasal mucous membrane. Reconstruction with iliac crest bone block

None stated

CT MRI

Complete radical resection

Recurrence at 3 months *Malignant transformation seen on histology

None stated

ND


No recurrence at 3 months follow up

3. Intraoral 4. Orbital floor destruction (25) Li Y, 2013 [12] China

36

40 Y

F

Bilateral Size: ND

1. Nasal Cavity


2. Maxillary sinus

2. Bloody rhinorrhoea

3. Ethmoid sinus (26) Li GY 2013 [9] China

(27) Moon, 2014 [19] Korea

37

38

23 Y

9M

M

F

Left 3.2 × 2.5 cm

Right Size: ND

1. Left Lacrimal Sac

2. Extension to lacrimal sac & left orbit

2. Proptosis

3. Ethmoid sinus

3. Lateral displacement of globe

1. Nasal cavity

1. Incomitant esotropia of right eye (inability to abduct right eye) No nasal symptoms

None stated

CT MRI

Surgery and care undertaken in another hospital

ND Surgery and care undertaken in another hospital

1. Recurrent sinusitis

None stated

CT MRI

Surgical resection


2. Maxillary sinus 3. Erosion of orbital wall 4. Erosion of cribriform plate

(28) Wang T, 2014 [38] China (2 cases)

39

5Y

M

Right 2.5 × 3.6 × 4.3 cm

1. Nasal cavity 2. Ethmoid sinus

Page 9 of 14

1. Naval cavity



40

(29) Obidan, 2014 [39] Saudi Arabia

41

(30) Stewart, 2014 [13] USA **4 patients previously reported by Priest et al. 2010 [27] (4 new cases)

-

-

6W

F

14 Y Size: ND

M

7 Y**

M

15 Y**

F



1. Nasal cavity


2. Pressure remodelling of adjacent bones

2. Watery rhinorrhoea



Initially unilateral, then bilateral

ND

1. Nasal Congestion

Bilateral

ND

Left 2.6 × 3.4 × 3.9 cm

Bilateral

None stated

CT MRI

Surgical resection


1. PPB

CT

Surgical endoscopic resection

ND

Surgical resection

Multiple recurrences

Surgical resection

No recurrence

Surgical resection

No recurrence

2. Decreased sense of smell 1. PPB 2. Lung cysts 1. Chronic Sinusitis

1. PPB

2. Facial Pain 3. Nasal Congestion

2. Sertoli-Leydig Cell Ovarian Tumour

-

10 Y**

F

Bilateral

ND

1. Nasal congestion

1. PPB

-

11 Y**

M

Right

ND

1. Nasal Congestion

1. PPB

42

8Y

M

ND Size: ND

ND

1. ND

1. PPB

Surgical resection

No recurrence

ND

Surgical resection

No recurrence

ND

Surgical resection

No recurrence

2. Pulmonary cysts in utero



3. Jejunal Polyps 43

13 Y

F

Bilateral Size: ND

ND

1. ND

1. PPB 2. Thyroid Papillary carcinoma 3. Sertoli-Leydig tumour

44

8Y

M

Bilateral Size: ND

ND

1. Chronic Sinusitis

1. PPB

ND

Surgical resection

No recurrence

45

6Y

F

ND Size: ND

ND

ND

1. PPB

ND

Surgical resection

No recurrence

ND

Surgical resection

Recurrence at 4 years

2. Left cystic nephroma 3. Small bowel loop 46

21 Y

F

Right Size: ND

ND

1. Nasal Congestion

1. PPB

2. Septal deviation

2. Sertoli-Leydig Tumour

Page 10 of 14

(31) Chandra 2014 [40] India

(32) Mason 2015 UK

47

48

12 Y

49 Y

M

M

Right Size: ND

Right 0.5 × 2 × 2 cm

3. Nasal Obstruction (at recurrence)

3. Multi-nodular goitre

1. Nasal cavity


None stated

CT MRI

Surgical excision

2. Ethmoid sinus

2. Proptosis



3. Right facial pain

1. Nasal cavity

1. Nasal mass

None stated

None

Surgical excision


Y Years, M Months, D Days, M Male, F Female, ND not documented, PPB Pleuropulmonary blastoma, CT Computed Tomography, MRI Magnetic Resonance Imaging



Page 11 of 14


NCMH are typically seen as non-encapsulated, poorly defined masses often with cystic components [15]. Magnetic resonance imaging (MRI) of NCMH demonstrates a heterogeneous mass on T1 weighted images and T2 weighted images show the presence of cystic components. MRI also has the advantage of superior tissue characterisation and delineation of invasion of adjacent structures in comparison to CT [16]. Due to rarity of NCMH, even after thorough clinical and radiographic examination NCMH can be misdiagnosed, and differential diagnoses include: inverted papilloma, aneurysmal bone cysts or ossifying fibromas, nasoethmoidal encephalocoele, chondrosarcoma, nasal lymphoma, nasal glioma and rhabdomyosarcoma. Histopathological analysis following surgical resection is therefore needed for accurate diagnosis. Patients with NCMH most commonly present with symptoms of nasal obstruction, nasal mass, or eye signs, which reflects the involvement of NCMH in the nasal passages and orbit. Ophthalmic signs include signs of globe displacement such as strabismus, extropia, hypertelorism, proptosis, enophthalmus and ophthlmoplegia, direct results of the intra-ocular extension of NCMH or ocular compression by NCMH [17–26]. There has also been a report of a patient presenting with intra-oral symptoms due to involvement of the oral cavity [4]. Patients can therefore present to otolaryngology, ophthalmology or maxillo-facial departments and doctors in these specialties should be aware of this rare pathology. In our case, the patient did not complain of any cranial, ophthalmic or nasal symptoms but was aware of a slowly enlarging nasal mass. This is most likely due to the relatively small size of the tumour at the anterior nasal septum which did not obstruct the nasal passage. The aetiology of NCMH is thought to be due to an underlying genetic predisposition therefore accounting for the early presentation in the majority of cases. Priest et al. and Stewart et al. investigated patients with both NCMH and the rare paediatric dysembryonic sarcoma of the lung and pleura: pleuropulmonary blastoma (PPB) [13, 27]. In patients with NCMH and PPB Stewart et al. found germline DICER1 mutations in 6 out of 8 evaluated patients, and somatic DICER1 mutations in 2 out of those 6 patients with germline mutations [13]. This recent finding has established genetic proof of NCMH tumour association with DICER1 mutations and Stewart et al. therefore feel that NCMH should be considered part of the DICER1 tumour spectrum. The DICER1 familial tumour susceptibility syndrome confers an increased risk most commonly for pleuropulmonary blastoma (PPB) but also ovarian sex cord-stromal tumours; Sertoli-Leydig cell tumor [SLCT], juvenile granulosa cell tumour [JGCT] and gynandroblastomas. Less commonly the DICER1 tumour spectrum includes: cystic nephroma (CN), and thyroid gland neoplasia,

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multinodular goitres [MNG], adenomas, or differentiated thyroid cancers. The rarest observed tumours in this spectrum, alongside NCMHs, are ciliary body medulloepithelioma (CBME), botryoid-type embryonal rhabdomyosarcoma (ERMS) of the cervix or other sites, renal sarcomas, pituitary blastomas, and pineoblastomas [28]. Eleven patients in our systematic review had previous PPB and five of these also had other DIECR1 tumours. Surgeons and physicians should therefore be aware of these disease associations and should be vigilant of a diagnosis of NCMH in patients presenting with sino-nasal or orbital symptoms who have a history of any of these tumours. Johnson et al. importantly also point out that due to its location, NCMH is more likely to present early in life than the other DICER1 tumours [29]. Surgeons and physicians should therefore either offer DICER1 mutation analysis if available, or ensure long-term follow up of these patients and be vigilant for associated tumours, as NCMH may be the ‘herald tumour’ of this disease spectrum. There are also cases in the literature of children, adolescents and adults with NCMH who have had an asymptomatic infancy [9, 11, 12, 14]. This may imply that there are non-genetic components to NCMH pathogenesis. Alternatively it may simply reflect the insidious growth of the tumour or that some NCMH patients may only exhibit the phenotype later in life. However as this is an extremely rare pathology with only very recent formal association with the DICER1 mutation, the majority of the 42 reported cases have not had formal DICER1 mutation analysis. Therefore an association or lack thereof in the non-tested cases cannot be inferred. Successful management of NCMH entails complete resection in order to prevent recurrence. A complete excision however is not always technically feasible, especially in cases of intracranial extension of NCMH. An incomplete resection poses the risk of recurrence as well as the possibility of continued tumour growth and progressive symptoms. Nine patients in this systematic review were found to have disease recurrence, most likely from incomplete surgical excision.

Conclusions We present an unusual case of NCMH in an adult without nasal obstructive symptoms due to the anatomical location of the NCMH attached to the nasal septum. A systematic review of the literature has highlighted that presentation is mostly related to tumour location, with nasal mass, nasal obstruction and ophthalmic signs being the most common forms of presentation. The majority of patients presenting with NCMH are children and infants below the age of one, but there have now been a few adult cases of presentation. Surgical resection is the treatment of choice with low recurrence rates in the


majority of cases. There has only been one reported case of malignant transformation and NCMH is still considered a benign tumour. NCMH’s association with the DIECR1 mutation has very recently been established and therefore in light of this any patient with a DICER1-related tumour spectrum and new nasal or orbital symptoms should raise the suspicion of NCMH. Furthermore surgeons should subsequently be vigilant for associated DICER1 related tumours, as due to their location NCMHs may be the ‘herald tumour’ for this disease spectrum. This case and systematic review highlights the fact that NCMH can mimic other benign and malignant lesions and that surgeons and physicians should be aware of rare pathologies accounting for nasal masses.

Consent Written consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the editor-in-chief of this journal.

2.

3.

4.

5.

6. 7. 8.

9.

10.

11.

12. Abbreviations NCMH: Nasal chondromesenchymal hamartoma; EMBASE: Excerpta medica database; CT: Computed tomography; MRI: Magnetic resonance imaging; PPB: Pleuropulmonary blastoma; SLCT: Sertoli-leydig cell tumour; JGCT: Juvenile granulosa cell tumour; CN: Cystic nephroma; MNG: Multinodular goitres; CBME: Ciliary body medulloepithelioma; ERMS: Embryonal rhabdomyosarcoma; DICER1: is not an abbreviation, but the name of gene located on chromosome 14 at position q32.13. Competing interests The authors declare that they have no competing interests.

13.

14.

15. 16.

Authors’ contributions Contribution to conception and design: KM, AN, PC. Contribution to acquisition of data, analysis and interpretation: KM, AN, ET. Involved in drafting the manuscript & revising it critically: KM, AN, ET, PC. All authors read and approved the final manuscript. Authors’ information KM is a clinical teaching fellow with Barts and The London School of Medicine and Dentistry. ET is a clinical teaching fellow with Barts and The London School of Medicine and Dentistry AN is a junior registrar in ENT surgery in the London Deanery. PC is a locum consultant at a regional teaching hospital where the case was encountered.

17.

18.

19.

20. 21.

Acknowledgements Thanks to Dr Ian Seddon (Consultant Histopathologist, Colchester Hospital University NHS Foundation Trust) for providing the histopathology images. 22. Author details 1 Barts and The London School of Medicine and Dentistry, The Blizard Institute of Cell and Molecular Science, 4 Newark Street, Whitechapel, E1 2AT London, UK. 2 Colchester Hospital University NHS Foundation Trust, Colchester, UK.

23. 24.

Received: 20 January 2015 Accepted: 1 June 2015 25. References 1. Moher D, Liberati A, Tetzlaff J, Altman DG, Group P. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. J Clin Epidemiol. 2009;62(10):1006–12.

26.

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